Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd2 |
A |
G |
7: 78,973,278 (GRCm39) |
M86V |
probably benign |
Het |
Acin1 |
C |
A |
14: 54,891,351 (GRCm39) |
|
probably benign |
Het |
Aebp2 |
T |
A |
6: 140,599,984 (GRCm39) |
|
probably benign |
Het |
Akap13 |
A |
G |
7: 75,258,732 (GRCm39) |
E452G |
probably damaging |
Het |
Amz1 |
T |
C |
5: 140,738,194 (GRCm39) |
S184P |
possibly damaging |
Het |
Armh4 |
T |
A |
14: 50,007,893 (GRCm39) |
T527S |
probably damaging |
Het |
Ccdc83 |
A |
T |
7: 89,875,986 (GRCm39) |
L295* |
probably null |
Het |
Cpsf7 |
A |
T |
19: 10,517,001 (GRCm39) |
I368F |
probably damaging |
Het |
Csf1r |
G |
A |
18: 61,252,078 (GRCm39) |
C520Y |
probably damaging |
Het |
Dapk1 |
A |
G |
13: 60,867,498 (GRCm39) |
D235G |
probably benign |
Het |
Ercc1 |
G |
A |
7: 19,081,057 (GRCm39) |
|
probably benign |
Het |
Fktn |
T |
C |
4: 53,720,201 (GRCm39) |
S72P |
probably damaging |
Het |
Frem2 |
C |
A |
3: 53,452,923 (GRCm39) |
V2189F |
possibly damaging |
Het |
Gm10845 |
G |
T |
14: 80,100,563 (GRCm39) |
|
noncoding transcript |
Het |
Hk1 |
C |
A |
10: 62,151,319 (GRCm39) |
K10N |
probably damaging |
Het |
Lama1 |
A |
G |
17: 68,111,513 (GRCm39) |
M2255V |
probably benign |
Het |
Lrsam1 |
G |
T |
2: 32,845,203 (GRCm39) |
T104K |
possibly damaging |
Het |
Myh6 |
T |
A |
14: 55,199,565 (GRCm39) |
I249F |
probably damaging |
Het |
Myo7a |
G |
A |
7: 97,751,881 (GRCm39) |
T54M |
probably damaging |
Het |
Or52ae7 |
T |
C |
7: 103,119,278 (GRCm39) |
S11P |
probably damaging |
Het |
Or5k15 |
A |
C |
16: 58,710,242 (GRCm39) |
C114G |
probably benign |
Het |
Osbpl8 |
T |
A |
10: 111,105,280 (GRCm39) |
I245N |
possibly damaging |
Het |
Pfkp |
A |
G |
13: 6,671,025 (GRCm39) |
S135P |
probably damaging |
Het |
Phf20l1 |
C |
T |
15: 66,476,686 (GRCm39) |
T260I |
possibly damaging |
Het |
Pole |
T |
A |
5: 110,485,071 (GRCm39) |
I395K |
possibly damaging |
Het |
Ppp6r2 |
T |
G |
15: 89,149,361 (GRCm39) |
C216W |
probably damaging |
Het |
Pramel7 |
C |
T |
2: 87,320,415 (GRCm39) |
A293T |
probably benign |
Het |
Rpl11 |
G |
A |
4: 135,778,454 (GRCm39) |
|
probably benign |
Het |
Scamp3 |
G |
A |
3: 89,089,234 (GRCm39) |
|
probably null |
Het |
Setbp1 |
T |
C |
18: 78,903,137 (GRCm39) |
R177G |
probably damaging |
Het |
Sh2b3 |
G |
T |
5: 121,966,549 (GRCm39) |
|
probably benign |
Het |
Tbc1d30 |
A |
G |
10: 121,130,617 (GRCm39) |
F271S |
probably damaging |
Het |
Tpo |
T |
C |
12: 30,153,151 (GRCm39) |
E401G |
possibly damaging |
Het |
Zdhhc13 |
T |
C |
7: 48,458,589 (GRCm39) |
Y308H |
probably damaging |
Het |
Zfp112 |
C |
T |
7: 23,825,798 (GRCm39) |
H589Y |
probably damaging |
Het |
Zmiz1 |
T |
C |
14: 25,636,434 (GRCm39) |
S140P |
probably damaging |
Het |
|
Other mutations in Cd209c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Cd209c
|
APN |
8 |
3,990,339 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01340:Cd209c
|
APN |
8 |
3,995,892 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02682:Cd209c
|
APN |
8 |
3,990,324 (GRCm39) |
missense |
probably damaging |
0.99 |
R1311:Cd209c
|
UTSW |
8 |
3,995,908 (GRCm39) |
start codon destroyed |
probably benign |
|
R1859:Cd209c
|
UTSW |
8 |
3,994,953 (GRCm39) |
missense |
probably benign |
|
R4375:Cd209c
|
UTSW |
8 |
4,004,635 (GRCm39) |
exon |
noncoding transcript |
|
R4377:Cd209c
|
UTSW |
8 |
4,004,635 (GRCm39) |
exon |
noncoding transcript |
|
R4769:Cd209c
|
UTSW |
8 |
3,994,953 (GRCm39) |
missense |
probably benign |
|
R4786:Cd209c
|
UTSW |
8 |
3,995,698 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4841:Cd209c
|
UTSW |
8 |
3,995,905 (GRCm39) |
missense |
probably benign |
0.00 |
R4842:Cd209c
|
UTSW |
8 |
3,995,905 (GRCm39) |
missense |
probably benign |
0.00 |
R4869:Cd209c
|
UTSW |
8 |
3,994,077 (GRCm39) |
missense |
probably benign |
0.00 |
R5333:Cd209c
|
UTSW |
8 |
3,994,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R5835:Cd209c
|
UTSW |
8 |
3,995,699 (GRCm39) |
missense |
probably benign |
0.01 |
R6369:Cd209c
|
UTSW |
8 |
3,994,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R6497:Cd209c
|
UTSW |
8 |
3,994,122 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6591:Cd209c
|
UTSW |
8 |
3,995,680 (GRCm39) |
missense |
probably benign |
0.14 |
R6691:Cd209c
|
UTSW |
8 |
3,995,680 (GRCm39) |
missense |
probably benign |
0.14 |
R7181:Cd209c
|
UTSW |
8 |
3,995,712 (GRCm39) |
missense |
probably benign |
0.01 |
R8067:Cd209c
|
UTSW |
8 |
3,995,700 (GRCm39) |
missense |
probably benign |
0.12 |
R8701:Cd209c
|
UTSW |
8 |
3,995,892 (GRCm39) |
missense |
probably benign |
0.00 |
R9722:Cd209c
|
UTSW |
8 |
3,995,905 (GRCm39) |
missense |
probably benign |
0.00 |
|